Canonical Allele Identifier: CA1603609047

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177404246G= , CM000667.2:g.177404246G= GRCh38
NC_000005.9:g.176831247G= , CM000667.1:g.176831247G= GRCh37
NC_000005.8:g.176763853G= NCBI36
NG_007568.1:g.10331C= , LRG_145:g.10331C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696192.1:c.*634C= (F12) ENSP00000512476.1:n.*634C=
ENST00000696193.1:c.*1338C= (F12) ENSP00000512477.1:n.*1338C=
ENST00000696194.1:c.*558C= (F12) ENSP00000512478.1:n.*558C=
ENST00000696195.1:n.3771C= (F12)
ENST00000696200.1:n.1071C= (F12)
ENST00000696201.1:c.968C= (F12) ENSP00000512482.1:p.Pro323=
ENST00000253496.4:c.968C= (F12) MANE Select ENSP00000253496.3:p.Pro323=
ENST00000253496.3:c.968C= (F12) ENSP00000253496.3:p.Pro323=
ENST00000502598.5:c.-45+720G= (GRK6) ENSP00000422873.1:n.-45+720G=
ENST00000502854.5:n.227C= (F12)
ENST00000503736.1:n.340C= (F12)
ENST00000510358.5:n.227C= (F12)
NM_000505.3:c.968C= , LRG_145t1:c.968C= (F12) NP_000496.2:p.Pro323=
XM_011534461.1:c.968C= (F12) XP_011532763.1:p.Pro323=
XM_011534462.1:c.632C= (F12) XP_011532764.1:p.Pro211=
XM_011534462.2:c.632C= (F12) XP_011532764.1:p.Pro211=
XM_017009773.2:c.1416+7172G= (SLC34A1) XP_016865262.1:n.1416+7172G=
NM_000505.4:c.968C= (F12) MANE Select NP_000496.2:p.Pro323=